WO2017146309A1 - Nouvelle utilisation de l'eupatiline comme composition pharmaceutique pour prévenir et traiter la fibrose via la capacité de celle-ci à inhiber la transition épithélio-mésenchimateuse - Google Patents

Nouvelle utilisation de l'eupatiline comme composition pharmaceutique pour prévenir et traiter la fibrose via la capacité de celle-ci à inhiber la transition épithélio-mésenchimateuse Download PDF

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WO2017146309A1
WO2017146309A1 PCT/KR2016/005960 KR2016005960W WO2017146309A1 WO 2017146309 A1 WO2017146309 A1 WO 2017146309A1 KR 2016005960 W KR2016005960 W KR 2016005960W WO 2017146309 A1 WO2017146309 A1 WO 2017146309A1
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fibrosis
pharmaceutical composition
present
emt
eupatillin
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윤병수
김한수
윤호섭
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(주)오스티오뉴로젠
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365—Lactones
    • A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A61K9/0021—Intradermal administration, e.g. through microneedle arrays, needleless injectors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2121/00—Preparations for use in therapy

Definitions

  • the present invention relates to a new use of eupatillin as an agent for the prevention and treatment of fibrosis, and in particular, as the present invention newly discovers that eupatilin can inhibit epithelial mesenchymal transition (ETM). It relates to a new use utilizing the activity as an agent for the prevention and treatment of fibrosis.
  • ETM epithelial mesenchymal transition
  • Fibrosis is a disease in which excessive fibrous connective tissue is formed in organs or tissues during regeneration or reaction, which is in contrast to the formation of normal fibrous tissue. If the fibrous connective tissue is excessively formed in the organ or tissue, the tissue is hardened and the influx of body fluids is reduced, and thus the original function cannot be sufficiently performed in vivo. Causes include injury, inflammation, burns, radiation, chemotherapy, lymphedema. The problem caused by fibrosis depends on the location of the fibrous connective tissue is formed, mainly liver, secretory organs, lungs, etc. are damaged. Fibrosis is typically idiopathic pulmonary fibrosis (IPF), myelo fibrosis, liver fibrosis and kidney fibrosis.
  • IPF idiopathic pulmonary fibrosis
  • Idiopathic pulmonary fibrosis is a chronically progressive interstitial pulmonary disease with poor disease progression and yet no proven treatment. Diagnosis is made when a biopsy of the lung reveals a honeycomb or irregular shape. Slow respiratory distress and death with hypoxia or myocardial infarction. To date, no clear cause has been proven, but various factors such as environment, virus, and heredity cause inflammation in the lungs. have.
  • Myelofibrosis is a disease in which the fibers of bone marrow tissue are over-developed, which lowers the function of making blood and changes in the number of red blood cells and white blood cells, and their actions. It is divided into idiopathic and secondary. Dual idiopathic symptoms include severe fibrotic hyperplasia and hypertrophy of systemic bone marrow, and nucleated red blood cells or weak granulocytes in peripheral blood. The cause is uncertain, and bone marrow poisoning and inflammation are thought to be the cause. Secondary manifestations occur during the course of leukemia, malignant lymphoma, cancer metastasis, and chemical poisoning. Effective therapeutics have not yet been developed.
  • Liver fibrosis is also called cirrhosis.
  • Chronic inflammation causes normal liver tissue to turn into fibrotic tissue, such as regenerative nodules, resulting in decreased liver function.
  • Treatment is aimed at delaying the progression of symptoms as much as possible.
  • antiviral drugs are used, but if the causes are different, the effect is unknown.
  • Renal fibrosis is a progressive disease in which extracellular matrix accumulates and fibrosis occurs in the kidney. It is characterized by glomerulosclerosis and tubular interstitial fibrosis. Fibrosis of the kidneys causes side effects in kidney function. Causes include trauma, infection, surgery, environmental factors, chemicals, radiation exposure, and symptoms such as pain, urination problems, nausea and vomiting. Drugs or kidney transplants can be used to manage symptoms, but they also require the development of effective therapies.
  • Twist or Snail a major regulator of epithelial mesenchymal transition (EMT) plays an important role in renal fibrosis.
  • EMT epithelial mesenchymal transition
  • Lovisa et al. It has been suggested to play an important role.
  • EMT refers to a phenomenon in which normal cells are genetically reprogrammed in the form of mesenchymal cells that are likely to move due to an intermediate cytoskeletal change as they progress to tumor cells. Therefore, it is thought that inhibiting the expression of EMT-related proteins can inhibit the metastasis and proliferation of tumors. Therefore, various researchers are conducting studies related to these EMTs to develop tumor therapeutics. About 20 regulators such as Twist, Snail, Slug, E-cadherin, collagen are known.
  • DEC2 is a transcription inhibitor of Twist, a regulator of EMT, and that inhibiting its expression activates EMT and converts it into a malignant tumor. Sato et al. Also reported that DEC2 inhibits the expression of Slug, a regulator of EMT, and thus suppresses malignant tumoration induced by TGF- ⁇ . In addition, various researchers have reported that modulators of EMT, such as DEC2, are associated with cancer metastasis.
  • eupatillin is a larvae ( Artemisia , Artemisia) asiatica ) is known as a component, and has been mainly studied the anticancer effect.
  • the inventors have explored the potential of eupatini as a therapeutic agent for fibrosis by using the association between EMT and fibrosis. As a result, it was newly revealed through the cell model and the animal model that eupatillin can suppress EMT. Accordingly, it was confirmed that eupatillin effectively inhibits the fibrosis of organs or tissues by activation of EMT, thus completing the present invention. Was done.
  • the main object of the present invention is to provide a new use of eupatilin as an agent for the prevention and treatment of fibrosis.
  • Another object of the present invention is to provide a new pharmaceutical composition for the prevention and treatment of fibrosis.
  • the present invention provides a pharmaceutical composition for the prevention and treatment of diseases caused by fibrosis, i.e., fibrosis of organs or tissues of a living body, which contains eufatlin as an active ingredient.
  • the pharmaceutical composition of the present invention is a group consisting of idiopathic pulmonary fibrosis, myelo fibrosis, liver fibrosis and kidney fibrosis among diseases caused by fibrosis of organs or tissues of a living body. It may be particularly effective in the prevention and treatment of the disease selected from among.
  • the pharmaceutical composition of the present invention can inhibit the fibrosis of organs or tissues of a living body by inhibiting the activation of Epithelial Mesenchymal Transition (EMT) (hereinafter abbreviated as 'EMT').
  • EMT Epithelial Mesenchymal Transition
  • the present invention provides a method for preventing or treating a disease caused by fibrosis of organs or tissues of a living body, which is characterized by administering eufatlin to an animal.
  • the method of the present invention is selected from the group consisting of idiopathic pulmonary fibrosis, myelo fibrosis, liver fibrosis and kidney fibrosis among diseases caused by fibrosis of organs or tissues of a living body. It may be particularly effective in the prevention and treatment of diseases.
  • Eupatillin as an active ingredient of the pharmaceutical composition of the present invention is represented by the following formula.
  • eupatillin can inhibit EMT.
  • EMT refers to a phenomenon in which normal cells are genetically reprogrammed in the form of mesenchymal cells that are likely to move due to an intermediate cytoskeletal change as they progress to tumor cells.
  • the effect of inhibiting fibrosis of eupatini was demonstrated through experiments using animal models or cell models that induced fibrosis through specific treatment.
  • Bleomycin is a substance that induces pulmonary fibrosis, and fibrosis proceeded only by treatment with bleomycin, and since eufitillin inhibited this fibrosis, it means that eupatillin effectively inhibits fibrosis.
  • hepatic mesenchymal stem cells derived from rat liver tissues were prepared, and TGF- ⁇ , which is known to induce activation of EMT, was treated to activate EMT and thereby differentiate into fibroblasts.
  • TGF- ⁇ which is known to induce activation of EMT
  • eupatillin was found to effectively inhibit the differentiation into these fibroblasts.
  • Col1 type 1 collagen
  • Vim vimentin
  • Twist which are known as markers of EMT
  • eupatillin increases the expression of DEC2 in rat bone marrow cells. Since DEC2 is a factor that inhibits transcription of Twist, a regulator of EMT, these results suggest that eupatin may inhibit the activation of EMT. it means.
  • the pharmaceutical composition of the present invention may contain 0.1 to 90% by weight of eufatlinin based on the weight of the total composition.
  • the pharmaceutical composition of the present invention can be administered orally or parenterally during clinical administration and intraperitoneal injection, rectal injection, subcutaneous injection, intravenous injection, intramuscular injection, intrauterine dural injection, cerebrovascular injection during parenteral administration. Or by intrathoracic injection, and can be used in the form of general pharmaceutical formulations.
  • composition of the present invention may be used alone or in combination with methods using surgery, radiation therapy, hormone therapy, chemotherapy and biological response modifiers.
  • the daily dosage of the pharmaceutical composition of the present invention may be about 0.0001 to 100 mg, preferably 0.001 to 10 mg per 1 kg of body weight, based on the eupatin contained in the composition, and may be administered once to several times a day.
  • the range varies depending on the patient's weight, age, sex, health condition, diet, time of administration, method of administration, rate of excretion and severity of the disease.
  • parenteral formulations which may be formulated using conventional diluents or excipients such as fillers, extenders, binders, wetting agents, disintegrating agents, surfactants, and the like.
  • Formulations for parenteral administration may include sterile aqueous solutions, non-aqueous solvents, suspensions, emulsions, lyophilized preparations, suppositories.
  • non-aqueous solvent and the suspension solvent propylene glycol, polyethylene glycol, vegetable oil such as olive oil, injectable ester such as ethyl oleate, and the like can be used.
  • base of the suppository witepsol, macrogol, tween 61, cacao butter, laurin butter, glycerogelatin and the like can be used.
  • the pharmaceutical composition of the present invention may further contain at least one active ingredient exhibiting the same or similar function in addition to eupatillin.
  • the prophylactic or therapeutic method of the present invention can be used in humans or animals other than humans.
  • the administration method and dosage of eupatillin may be applied according to the administration method and dosage of the pharmaceutical composition.
  • the pharmaceutical composition of the present invention can effectively inhibit the activation of EMT by containing eupatillin as an active ingredient, and thus can effectively inhibit the fibrosis of organs or tissues induced by the activation of EMT.
  • eupatillin as an active ingredient
  • the method for preventing or treating fibrosis of the present invention due to the activity of the above-described eupatini, it is possible to effectively prevent or treat fibrosis.
  • 1 is a chemical structure of eupatillin as an active ingredient of the pharmaceutical composition of the present invention.
  • Figure 2 is a graph showing the effect of increasing the DEC2 expression of eupatini as an active ingredient of the pharmaceutical composition of the present invention.
  • Figure 3 shows the fibrosis inhibitory effect of eupatillin, the active ingredient of the pharmaceutical composition of the present invention, one mouse in each experimental group lungs tissue masson's trichrome staining photograph taken under the microscope.
  • Normal control group normal mice raised without administration of bleomycin and eupatillin
  • bleomycin-administered group mice induced pulmonary fibrosis by bleomycin administration
  • bleomycin + eupatylin-administered group induce pulmonary fibrosis by administration of bleomycin Mice administered with eupatillin (40 ⁇ g).
  • Figure 4 shows the results of the IHC analysis of ONGHEPA1 cells used to confirm the effect of eupatini, it can be seen that this cell line is not hepatocytes as cells differentiated from ectoderm or endoderm. Left: IHC results using anti-GATA4 antibody, right: IHC results using anti-CK-18 antibody.
  • FIG. 5 shows the results of FACS analysis of the ONGHEPA1 cell line used to confirm the effect of eupatini
  • ONGHEPA1 is a mesenchymal stem cell of the liver expressing the biofilm proteins CD29, CD44, CD71 and CD106.
  • Figure 6 shows the experimental results of the fibrosis inhibitory effect of eupatillin, the active ingredient of the pharmaceutical composition of the present invention, micrographs according to the culture time (6 hours, 12 hours, 24 hours, 48 hours elapsed time) and treatment of ONGHEPA1 cells It is shown.
  • Normal control group control group cultured ONGHEPA1 cells without treatment
  • TGF- ⁇ treatment group experimental group cultured ONGHEPA1 cells by adding TGF- ⁇ to the culture medium
  • TGF- ⁇ + eupatin treatment group TGF- ⁇
  • Figure 7 shows the experimental results of the fibrosis inhibitory effect of eupatillin, the active ingredient of the pharmaceutical composition of the present invention, showing the real-time RT-PCR analysis of the expression patterns of Col1, Vim and Twist according to the treatment of ONGHEPA1 cells It is a graph. Cont: Control, cultured ONGHEPA1 cells without treatment, Eup. : Experimental group cultivated ONGHEPA1 cells by adding eupatini to the culture medium, TGF ⁇ : Experimental group cultivated ONGHEPA1 cells by adding TGF- ⁇ to the culture medium, TGF ⁇ + Eup. : Experimental group in which ONGHEPA1 cells were cultured by adding TGF- ⁇ and eupatillin to the culture medium.
  • DEC2 is known as a transcription inhibitor of Twist and Slug, which are regulators of epithelial mesenchymal transition (ETM).
  • ETM epithelial mesenchymal transition
  • Rat bone marrow cells were activated by treatment with macrophage-colony stimulating factor (M-CSF) and receptor activator of NF ⁇ B (RANNKL) ligands (RANKL). After 4 days of incubation, the expression pattern of DEC2 was confirmed.
  • M-CSF macrophage-colony stimulating factor
  • RNKL receptor activator of NF ⁇ B ligands
  • Example 1 it was confirmed that eupatillin increases the expression of DEC2, thereby confirming the possibility that eupatillin will inhibit fibrosis. Based on this, a real animal model was used to determine whether eupatini could actually inhibit tissue fibrosis.
  • mice Five-week-old male C57BL / 6J mice (18.2-20.5 g in weight) (KOATECH, Korea) were used as experimental animals. The experimental animals were divided into five groups in each group as shown in Table 1 below.
  • the experimental animals used polysulfone material, 369L x 156W x 132H (mm) (EU, USA, UK GL compliance) standard breeding box in SPF (Specific Pathogen Free), BSL (Bio Safety Level) Level 2 facility. Breeding was done. The number of animals per breeding box was 2 to 3 in the quarantine / purifying period and 2 to 3 in the testing period. The temperature was 22 ⁇ 2 °C, the relative humidity was 50.0 ⁇ 15.0%, the ventilation frequency was 10-20 times / hour, and the contrast was Cycle (lighting time) 12 hours / day (07:00 ⁇ 19:00), was bred under the conditions of the illumination of 150 ⁇ 300 Lux.
  • Pulmonary fibrosis was performed by injecting a bleomycin solution directly into the lungs through trachea according to the intratracheal instillation (IT) method of Kremer et al., Laxer et al. And Berkman et al. That is, while inhalation of C57BL / 6J mice with 70% N 2 O, 30% O 2 gas and 1.5% isoflurane, the skin was cut in the foreground, the muscles were cleaned, the organs were exposed, and the organs were removed with ophthalmic surgical scissors. A little incision was made.
  • IT intratracheal instillation
  • bleomycin-dissolved distilled water was injected directly into the lungs through the incision. Immediately after injection, the incision skin was sutured, awakened from anesthesia, and housed in a general breeding cage.
  • the administration of bleomycin was performed using a video instillobot, and 12-day pulmonary fibrotic disease induction period was set by one administration of 40 ⁇ g / 50 ⁇ l of bleomycin-HCl.
  • Eupatillin was dissolved in DPBS buffer (containing 1% DMSO), and the dosage of eupatillin was 1 ml / kg, and the individual dose was calculated based on recent weight measurement. Twelve days after bleomycin administration, the group was forced nasal administration once a day (five times a week) for one week using a micropipette. Toxicity symptoms and mortality were observed for two to three days after eupatillin administration, but no abnormal symptoms were observed after administration of bleomycin and eupatillin.
  • mesenchymal stem cells were prepared and treated with TGF- ⁇ to confirm the effect of eupatillin in the process of inducing liver fibrosis.
  • HSC is closely related to liver fibrosis. HSC is converted into fibrotic cells and liver fibrosis is achieved by secreting various proteins involved in Epithelial Mesenchymal Transition (EMT).
  • EMT Epithelial Mesenchymal Transition
  • RT-PCR results It was confirmed that albumin negative ONGHEPA1 cell line is not hepatocytes. Note that HSCs are not hepatocytes and therefore do not express albumin.
  • IHC analysis result IHC was performed using anti-GATA4 and anti-CK-18 antibodies after fixation of ONGHEPA1 cell line, indicating that GATA4 and CK-18, ie endo / ectodermal markers, were expressed. This indicates that the ONGHEPA1 cell line is not hepatocytes (see FIG. 4).
  • FACS analysis result FACS was performed with MSC marker antibody to confirm whether ONGHEPA1 cell line is MSC of liver. CD29, CD44, CD71 and CD106 were expressed on the surface of the cells, confirming that ONGHEPA1 is MSC (see FIG. 5).
  • HSC liver fibrosis
  • HSCs are differentiated into several cells, one of which is fibroblasts. HSCs also secrete large amounts of extracellular matrix protein (ECM) between cells, slowing their movement. Collagen ⁇ 1 is the most abundant ECM protein.
  • ECM extracellular matrix protein
  • ⁇ SMactinin alpha smooth muscle actinin
  • ONGHEPA1 The fiberization characteristics of ONGHEPA1 were confirmed using the characteristics of HSC as described above.
  • the cells were treated with transforming growth factor beta (TGF- ⁇ ) at 6 hours, 12 hours, 24 hours, and 48 hours, and then observed at 24 hours and 48 hours. It was confirmed that significant fibrosis had progressed (see 'TGF- ⁇ treatment group' in FIG. 6).
  • TGF- ⁇ transforming growth factor beta
  • ONGHEPA1 cells The fibrosis properties of ONGHEPA1 cells were confirmed through 3-2, and experiments were performed to analyze the effects of eupatini.
  • TGF- ⁇ was treated to induce fibrosis, but eupatini was added to the culture at a concentration of 50 ⁇ M.
  • eupatini was added to the culture at a concentration of 50 ⁇ M.
  • the pharmaceutical composition of the present invention can effectively inhibit the activation of EMT by containing eupatillin as an active ingredient, and thus can effectively inhibit the fibrosis of organs or tissues induced by the activation of EMT. Therefore, the pharmaceutical composition of the present invention can be usefully used in the medicament for the prevention or treatment of fibrosis.

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Abstract

La présente invention concerne une nouvelle utilisation de l'eupatiline comme agent de prévention et de traitement contre la fibrose, et plus spécifiquement, étant donné qu'il a été récemment découvert au travers de la présente invention que l'eupatiline pouvait inhiber la transition épithélio-mésenchymateuse (TEM), la présente invention concerne une nouvelle utilisation de l'eupatiline comme agent de prévention et de traitement contre la fibrose via l'utilisation de cette activité de cette dernière. Une composition pharmaceutique fournie par la présente invention contient de l'eupatiline comme principe actif, et peut donc inhiber efficacement l'activation de la TEM, et en conséquence peut efficacement inhiber la fibrose d'organes ou de tissus induite par une activation de la TEM. Ou, selon une méthode pour prévenir ou traiter la fibrose, selon la présente invention, la fibrose peut être de façon efficace prévenue ou traitée au moyen de cette activité de l'eupatiline.
PCT/KR2016/005960 2016-02-22 2016-06-07 Nouvelle utilisation de l'eupatiline comme composition pharmaceutique pour prévenir et traiter la fibrose via la capacité de celle-ci à inhiber la transition épithélio-mésenchimateuse WO2017146309A1 (fr)

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KR10-2016-0020673 2016-02-22
KR20160020673 2016-02-22
KR10-2016-0032719 2016-03-18
KR20160032719 2016-03-18
KR20160062556 2016-05-23
KR10-2016-0062556 2016-05-23

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CN111836808A (zh) * 2018-02-27 2020-10-27 欧斯特奥纽罗根有限公司 用于预防、减轻或治疗纤维化或非酒精性脂肪性肝炎的新型化合物和包含其作为活性成分的组合物
CN112353792A (zh) * 2020-10-29 2021-02-12 南通大学 异泽兰黄素在制备预防或治疗酒精性肝病药物中的应用

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KR101991454B1 (ko) * 2017-05-23 2019-06-20 차의과학대학교 산학협력단 크로메논 유도체를 유효성분으로 포함하는 폐섬유화 예방 또는 치료용 약제학적 조성물
CN109758449A (zh) * 2019-02-28 2019-05-17 天津国际生物医药联合研究院 杨梅素在制备用于治疗肺纤维化疾病的药物中的应用
WO2021015218A1 (fr) * 2019-07-24 2021-01-28 国立大学法人九州大学 Prévention ou traitement d'une fibrose ciblant le facteur associé à la transcription
KR102091464B1 (ko) * 2019-08-30 2020-03-20 (주)오스티오뉴로젠 항염증용 조성물
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